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Operation Supervisor Job Indonesia,  

MSD (company)

Posted on : 10 April 2017

Project Description

Operation Supervisor-MAN003656


1. Principle Objective of Position
Responsible for the manufacturing process, packaging the drugs into the finished product and ready to be distributed to the market in accordance with the GMP standards (QMS - Core Requirement, Prod. Monograph, IMPs) and Safety (GSE, Permenaker, etc.), so the highest quality product can be produced and meet the standards that have been set by PT. MSD Pharma Tbk.

2. Major Duties / Responsibilities

Responsible for implementing the company VISION: cost, quality, customer service and safety.

Supervise the process of drug manufacturing, packaging the drugs into the finished product in order to be appropriate with the guidance of manufacturing and packaging process.

Ensure that the label and the material used was in accordance with the Shop Floor Paper.

Convince the workplace, the packaging line, the machines used is clean and free from the previous products.

The separation of the room and packaging line along with the identity in order to avoid contamination or mix - up.

Ensure that In- Process Control performed during the manufacturing process and packaging occur

Will be involved as a member of Team Plant Inspection, MRB, Investigation of Product Complaint if necessary.

Conduct examinations that the equipment, rooms and facilities used already have clean identity and it must be really clean in accordance with the status / identity listed.

Oversight the step - a critical step or another step that required for the manufacturing process of drugs and drug packaging (material receipt, set up the machine, filling process, stripping, printing, labeling, etc.).

Reviewing / verify the completeness of batch record as the result of drug manufacturing and packaging process step by step, that have been set in the instructions of drug manufacturing process and packaging process and provide a reason if any mismatch or deviation found, as stated in the instructions of manufacture of drugs and packaging.

Responsible for the correctness of reconciliation process / recalculation of drug usage and the quantity of material used in order to ensure that the drug and the existing material only used for those products.

Ensure that the equipments / production machine, supporting equipment, and supporting facilities are still in the range of calibration at the time will be used for the production process.

Setting up the Standards Yields and Standard Hours annually.

Avoid or reduce the product complaint, product reject, product re-call, product re-pack, and etc.

Participate on drug manufacturing process planning and packaging, and cooperate with the Buyer Planner department. Responsible for the implementation in the production and packaging departments and supervise / monitor the activities in every sub-department including personnel arrangements in order to be efficient and productive.

Participate for the preparation of Financial Plan Expenditure of Production and Packaging Department annually, and ensure the financial expenditure is in accordance with the predetermined plan and if there are deviations (over the predetermined plan) there must be a rational explanation (conducting control monthly).

Participate for preparing annual training program for operators, include: Back Up Training (cross-training program), GMP Training, Environment & Safety Training and others, and ensure its implementation, conduct evaluation (including cross-training program) and improving the operator ability.

Assist in the specifications plan of the new machines (Capital Plan) which will be purchased for the Production and Packaging department purposes.

Setting up the samples for clinical study, creating design for packaging material of the new products.


Bachelor Degree of Pharmacy / Pharmacist, or from another disciplines who have been trained for drug manufacturing and packaging process at least one year, or Pharmacist Assistant / Vocational High School of Pharmacy who has received training for drug manufacturing and packaging process at least 3 years.

The applicant also must have received GMP training, Process Validation, Statistical Process Control, Introduction of Manufacturing Drug Process Facilities and Packaging and Production Equipment, Management leadership, English knowledge and Computer Operation

Job: Manuf./Operations Generic Job Title:Mgr, Operations

Primary Location: APAC-ID-JW-Jawa Timur

Employee Status: Regular

Travel: Yes, 5 % of the Time

Number of Openings: 1

Company Trade Name:MSD

Job Segment: Manager, Pharmacy, Machinist, Clinical Research, Medical Research, Management, Healthcare, Manufacturing


Jawa Timur, ID

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